MeSH Browser

MeSH Supplementary: Glutathione synthetase deficiency
Unique ID: C536835
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536835
Entry Term(s): 5-oxoprolinemia; 5-oxoprolinuria; Deficiency of Glutathione Synthase; Deficiency of Glutathione Synthetase; Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to; Pyroglutamic Acidemia; Pyroglutamic aciduria
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; Glutathione Synthase / deficiency
Frequency: 28
Date of Entry: 2010/08/25
Revision Date: 2019/07/01

Glutathione synthetase deficiency MeSH Supplementary Concept Data 2024